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dc.contributor.authorIkeme, Jesse C.
dc.contributor.authorKatz, Ronit
dc.contributor.authorMuiru, Anthony N.
dc.contributor.authorEstrella, Michelle M.
dc.contributor.authorScherzer, Rebecca
dc.contributor.authorGarimella, Pranav S.
dc.contributor.authorHallan, Stein
dc.contributor.authorPeralta, Carmen A.
dc.contributor.authorIx, Joachim H.
dc.contributor.authorShlipak, Michael G.
dc.date.accessioned2023-04-18T06:57:40Z
dc.date.available2023-04-18T06:57:40Z
dc.date.created2022-12-22T11:29:39Z
dc.date.issued2022
dc.identifier.citationAmerican Journal of Hypertension. 2022, 35 (12), 1006-1013.en_US
dc.identifier.issn0895-7061
dc.identifier.urihttps://hdl.handle.net/11250/3063454
dc.description.abstractBACKGROUND Urine biomarkers of kidney tubule health may distinguish aspects of kidney damage that cannot be captured by current glomerular measures. Associations of clinical risk factors with specific kidney tubule biomarkers have not been evaluated in detail. METHODS We performed a cross-sectional study in the Systolic Blood Pressure Intervention Trial among 2,436 participants with a baseline estimated glomerular filtration rate (eGFR) <60 ml/min/1.73 m2. Associations between demographic and clinical characteristics with urine biomarkers of kidney tubule health were evaluated using simultaneous multivariable linear regression of selected variables. RESULTS Each standard deviation higher age (9 years) was associated with 13% higher levels of chitinase-3-like protein-1 (YKL-40), indicating higher levels of tubulointerstitial inflammation and repair. Men had 31% higher levels of alpha-1 microglobulin and 16% higher levels of beta-2 microglobulin, reflecting worse tubule resorptive function. Black race was associated with significantly higher levels of neutrophil gelatinase-associated lipocalin (12%) and lower kidney injury molecule-1 (26%) and uromodulin (22%). Each standard deviation (SD) higher systolic blood pressure (SBP) (16 mmHg) was associated with 10% higher beta-2 microglobulin and 10% higher alpha-1 microglobulin, reflecting lower tubule resorptive function. CONCLUSIONS Clinical and demographic characteristics, such as race, sex, and elevated SBP, are associated with unique profiles of tubular damage, which could reflect under-recognized patterns of kidney tubule disease among persons with decreased eGFR.en_US
dc.language.isoengen_US
dc.publisherOxford University Pressen_US
dc.titleClinical Risk Factors For Kidney Tubule Biomarker Abnormalities Among Hypertensive Adults With Reduced eGFR in the SPRINT Trialen_US
dc.title.alternativeClinical Risk Factors For Kidney Tubule Biomarker Abnormalities Among Hypertensive Adults With Reduced eGFR in the SPRINT Trialen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright © 2023 American Journal of Hypertensionen_US
dc.source.pagenumber1006-1013en_US
dc.source.volume35en_US
dc.source.journalAmerican Journal of Hypertensionen_US
dc.source.issue12en_US
dc.identifier.doi10.1093/ajh/hpac102
dc.identifier.cristin2096910
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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